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Sweden· SE-19940902000020

Famvir 250 mg Filmdragerad tablett

A medicinal product containing famciclovir, registered in Sweden by Phoenix Labs Unlimited Company.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedFamvir 250 mg Filmdragerad tablettATC—REGISTER NO.SE-19940902000020PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Famciclovir
Manufacturer
Phoenix Labs Unlimited Company
Country
Sweden (SE)
ATC code
—
Reimbursed
Not published by this register
Source register
Swedish Medical Products Agency (Sweden)
Last checked
October 1, 2026

Packs & prices · 1

  • se_varunummer
    19940902000020

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Famciclovir in 13 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All famciclovir products

Authorised across Europe · EMA

The same active substance is authorised in 16 EEA countries. Names it is sold under:

  • Austria · Famvir
  • Cyprus · Famvir
  • Germany · Famvir
  • Denmark · Famciclovir Viatris, Famvir
  • Spain · Famciclovir Normon, Famciclovir Pensa
  • Finland · Famvir
  • France · Oravir
  • United Kingdom (Northern Ireland) · Famciclovir Accord Healthcare, Famciclovir Cadila Pharmaceuticals (Europe)
  • Greece · Famcilet, Famvir
  • Hungary · Famvir
  • Ireland · Famciclovir Teva, Famvir
  • Iceland · Famvir
  • Italy · Coirgen, Famciclovir Mylan Generics
  • Malta · Famvir
  • Netherlands · Famciclovir Double-E Pharma, Famciclovir Sandoz
  • Slovakia · Famciclovir Teva

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Swedish Medical Products Agency (Sweden). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/93fa0e6a-5406-4476-b304-e1b017e13956
GET /v1/drugs/93fa0e6a-5406-4476-b304-e1b017e13956?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "source": "lakemedelsverket",
  "doc_types": [
    "PL",
    "SmPC"
  ],
  "se_npl_id": "19940902000020",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19940902000020",
  "product_doc_link": "https://docetp.mpa.se/LMF/Famvir%20film-coated%20tablets%20SmPC_09001bee807a27f4.pdf"
}

See everything about famciclovir.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.